To study and compare the effect of prednisolone acetate and nepafenac eyedrops in patients after surgery for cloudy lens (safed motiya)
Not Applicable
Completed
- Conditions
- Health Condition 1: H269- Unspecified cataract
- Registration Number
- CTRI/2023/01/049131
- Lead Sponsor
- Pt B D Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 43
Inclusion Criteria
1.Patients above 45 years of age with senile cataract undergoing phacoemulsification
2.Patients of either sex will be included
3.Patient willing to give written informed consent
Exclusion Criteria
1.Patients with presenile cataract, glaucoma, uveitis, complicated cataract, subluxated cataract, traumatic cataract or posterior segment pathology
2.Patients sensitive to aspirin and other related NSAIDs
3.Use of systemic or topical steroids within 2 weeks of surgery
4.Use of systemic or topical NSAIDs within 7 days of surgery
5.Patient with uncontrolled diabetes
6.Any intraoperative complication
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Change from baseline in Central corneal thickness post cataract surgery. <br/ ><br>2. Resolution of anterior chamber reaction. <br/ ><br>3. Improvement in visual acuity following cataract surgery.Timepoint: Patients will be evaluated at post-operative day 1, 1 week and 3 weeks. Any adverse drug reaction if occurs at any point in the study, has to be reported promptly and ADR monitoring to be done throughout the study.
- Secondary Outcome Measures
Name Time Method 1. Change from baseline Intraocular pressure following cataract surgery. <br/ ><br>2. Improvement in patient comfort post cataract surgery.Timepoint: Patients will be evaluated at post-operative day 1, 1 week and 3 weeks.